Recent advances in radical-mediated intermolecular (4+2) cycloaddition

被引:8
作者
Cai, Xue-Er [1 ]
Wang, Zi-Ying [1 ]
Tian, Wen-Chan [1 ]
Liu, Hongxin [2 ]
Wei, Wen-Ting [1 ]
Lei, Ke-Wei [1 ]
机构
[1] Ningbo Univ, Sch Mat Sci & Chem Engn, Ningbo 315211, Zhejiang, Peoples R China
[2] Wenzhou Univ, Coll Chem & Mat Engn, Wenzhou 325035, Zhejiang, Peoples R China
关键词
DIELS-ALDER REACTIONS; CASCADE CYCLIZATION; ANNULATION; CHEMISTRY; N-ENYNES; OXIDATION;
D O I
10.1039/d3ob00744h
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
(4 + 2) Cycloaddition plays an important role in the synthesis of versatile carbocyclic/heterocyclic compounds with its high atom- and step-economy. Additionally, with mild conditions and indispensable functional group compatibility, the radical reaction has been recognized as a useful tool in organic chemistry. Given the enormous impact of radical-mediated (4 + 2) cycloaddition processes and their promising applications, we summarize and highlight the recent works in this attractive area. On the basis of the types of radicals that initiate different (4 + 2) cycloaddition processes, we classify them into processes involving alkenyl cations or alkenyl radicals, aryl radicals, acyl radicals, alkyl radicals, and heteroatom radicals, and this review places special emphasis on the reaction design and mechanisms, which will stimulate future developments in radical-mediated intermolecular (4 + 2) cycloaddition.
引用
收藏
页码:6068 / 6082
页数:15
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